The fragile X syndrome. by Hirst, M, Knight, S, Bell, M, Super, M, Davies, K

“…This sequence appears to be both the source of the primary mutation causing the fragile X syndrome, apparently having its causative effect through the methylation of the FMR-1 HTF island and the region of cytogenetic fragility. …”

The fragile X syndrome. by Flannery, A, Hirst, M, Knight, S, Ritchie, R, Davies, K

Astrocytes in fragile X syndrome by Karo Talvio, Maija L. Castrén

Subjects: “…fragile X syndrome…”
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Screening for fragile X syndrome. by Murray, Cuckle, Taylor, Hewison

“…In 1991, the gene responsible for fragile X syndrome, a common cause of learning disability, was discovered. …”
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Fragile X syndrome: Current insight by Deepika Delsa Dean, Srinivasn Muthuswamy, Sarita Agarwal

Subjects: “…Fragile X syndrome (FXS)…”
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Impact of Fragile X Syndrome on Their Families by Concha Iriarte-Redín, Manuel Soriano-Ferrer, Beatriz Hidalgo-Alés

Subjects: “…fragile x syndrome…”
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Developmental studies in fragile X syndrome by Khaleel A. Razak, Kelli C. Dominick, Craig A. Erickson

“…Abstract Fragile X syndrome (FXS) is the most common single gene cause of autism and intellectual disabilities. …”
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Chloride imbalance in Fragile X syndrome by Kaleb Dee Miles, Caleb Andrew Doll

Subjects: “…fragile X syndrome…”
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The molecular basis of the Fragile X syndrome by Harem Othman smail

“…Fragile X syndrome is an X-linked mutation inheritance disorder. …”
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An “Omic” Overview of Fragile X Syndrome by Olivier Dionne, François Corbin

Subjects: “…fragile X syndrome…”
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Fragile X Syndrome and Targeted Treatments by Nattaporn Tassanakijpanich, Ana María Cabal-Herrera, Maria Jimena Salcedo-Arellano, Randi Jenssen Hagerman

Subjects: “…fragile x syndrome, fmr1, targeted treatment…”
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Modeling Fragile X Syndrome in Drosophila by Małgorzata Drozd, Małgorzata Drozd, Barbara Bardoni, Barbara Bardoni, Maria Capovilla, Maria Capovilla

Subjects: “…Fragile X Syndrome…”
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Auditory Processing in Fragile X Syndrome by Sarah E Rotschafer, Khaleel A Razak

Subjects: “…Fragile X Syndrome…”
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Molecular analysis of the fragile X syndrome. by Knight, S, Hirst, M, Davies, K

Prenatal diagnosis of fragile X syndrome. by Hirst, M, Knight, S, Davies, K, Cross, G, Ocraft, K, Raeburn, S, Heeger, S, Eunpu, D, Jenkins, E, Lindenbaum, R

Origins of the fragile X syndrome mutation. by Hirst, M, Knight, S, Christodoulou, Z, Grewal, P, Fryns, J, Davies, K

“…The fragile X syndrome is a common cause of mental impairment. …”

Molecular heterogeneity of the fragile X syndrome. by Nakahori, Y, Knight, S, Holland, J, Schwartz, C, Roche, A, Tarleton, J, Wong, S, Flint, T, Froster-Iskenius, U, Bentley, D

“…The fragile X syndrome is an X-linked disorder which has been shown to be associated with the length variation of a DNA fragment containing a CGG trinucleotide repeat element at or close to the fragile site. …”

Molecular studies of the fragile X syndrome. by Knight, S, Hirst, M, Roche, A, Christodoulou, Z, Huson, S, Winter, R, Fitchett, M, McKinley, M, Lindenbaum, R, Nakahori, Y

“…We have studied families segregating for the fragile X syndrome for the presence of amplification of the CGG repeat sequence adjacent to the HpaII Tiny Fragment (HTF) island in the FMR-1 gene. …”

Genotype prediction in the fragile X syndrome. by Hirst, M, Nakahori, Y, Knight, S, Schwartz, C, Thibodeau, SN, Roche, A, Flint, T, Connor, J, Fryns, J, Davies, K

“…The implications of these results for screening for the fragile X syndrome are discussed.…”

Fragile X syndrome: clinical and cytogenetic studies by TÊMIS MARIA FÉLIX, JOÃO MONTEIRO DE PINA-NETO

Subjects: “…fragile X syndrome…”
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